FDA UDI In Commercial Distribution 🇺🇸 United States

IVES-FANSLER RECTAL SPECULUM

DI: 00192896087941 · Model: 90-0180 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
IVES-FANSLER RECTAL SPECULUM
Primary DI
00192896087941
Version / Model
90-0180
Catalog Number
90-0180
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-17
Public Version
1
Public Version Date
2018-10-18
Public Version Status
New
Public Device Record Key
4390de70-470b-48d0-b833-8c416f7a96e8

Device Description

IVES-FANSLER RECTAL SPECULUM WITH RUBBER OBTURATOR FENESTRATED HANDLE

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
["Dry Heat Sterilization", "Moist Heat or Steam Sterilization"]

Product Codes

Code Name
FFQ SPECULUM, RECTAL

GMDN Terms

Code Name
35351 Rectal speculum

Identifiers

Type ID
Primary 00192896087941

Customer Contacts